Department of Genitourinary Oncology, Moffitt Cancer Center & Research Institute, Tampa, FL, 33612, USA.
Department of Integrated Mathematical Oncology, Moffitt Cancer Center & Research Institute, Tampa, FL, 33612, USA.
Nat Commun. 2017 Nov 28;8(1):1816. doi: 10.1038/s41467-017-01968-5.
Abiraterone treats metastatic castrate-resistant prostate cancer by inhibiting CYP17A, an enzyme for testosterone auto-production. With standard dosing, evolution of resistance with treatment failure (radiographic progression) occurs at a median of ~16.5 months. We hypothesize time to progression (TTP) could be increased by integrating evolutionary dynamics into therapy. We developed an evolutionary game theory model using Lotka-Volterra equations with three competing cancer "species": androgen dependent, androgen producing, and androgen independent. Simulations with standard abiraterone dosing demonstrate strong selection for androgen-independent cells and rapid treatment failure. Adaptive therapy, using patient-specific tumor dynamics to inform on/off treatment cycles, suppresses proliferation of androgen-independent cells and lowers cumulative drug dose. In a pilot clinical trial, 10 of 11 patients maintained stable oscillations of tumor burdens; median TTP is at least 27 months with reduced cumulative drug use of 47% of standard dosing. The outcomes show significant improvement over published studies and a contemporaneous population.
阿比特龙通过抑制 CYP17A(一种自身产生睾酮的酶)来治疗转移性去势抵抗性前列腺癌。按照标准剂量治疗,治疗失败(影像学进展)时出现耐药的中位时间约为 16.5 个月。我们假设将进化动力学纳入治疗中可以延长无进展时间(TTP)。我们使用Lotka-Volterra 方程开发了一个进化博弈论模型,其中包含三种相互竞争的癌症“物种”:雄激素依赖型、雄激素产生型和雄激素非依赖型。采用标准阿比特龙剂量的模拟实验表明,雄激素非依赖型细胞具有很强的选择优势,并且治疗迅速失败。适应性治疗使用患者特定的肿瘤动力学来告知治疗/停药周期,从而抑制雄激素非依赖型细胞的增殖并降低累积药物剂量。在一项试点临床试验中,11 名患者中有 10 名患者的肿瘤负担保持稳定波动;中位 TTP 至少为 27 个月,累积药物使用量减少 47%,为标准剂量的 47%。结果显示,与已发表的研究和同期人群相比,有显著改善。